Beachbody
SHAKEOLOGY - Greenberry
LNHPD
20893626
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
9
FDA consumer events
Certifications
0
none recorded
No authority-flagged excipients or recalls. · Every flag below links to the authority's published citation.
Supplement Facts
21 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Whey Protein Isolate ProteinUNII · 8617Z5FMF6 | 12851.0 milligrams | — |
| Smallanthus sonchifolius Yacon | 400.0 milligrams | — |
| Vitamin E UNII · H4N855PNZ1 | 12.46 mg AT | — |
| Vitamin E UNII · H4N855PNZ1 | 12.46 mg AT | — |
| 4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase | 256.0 FCC CU | — |
| beta-D-fructofuranoside fructohydrolase | 42.7 FCC SU | — |
| Beta-Galactosidase Beta-galactosidaseUNII · MEQ84W5J4Q | 342.0 FCC ALU | — |
| Amaranthus cruentus | 5.0 milligrams | — |
| Lepidium meyenii Maca | 855.0 milligrams | — |
| Camellia sinensis | 42.75 milligrams | — |
| Linum usitatissimum | 1050.0 milligrams | — |
| Chlorella vulgaris | 1000.0 milligrams | — |
| Arthrospira platensis Blue-Green Algae | 1000.0 milligrams | — |
| Copper UNII · 789U1901C5 | 800.0 micrograms | — |
| Chromium UNII · 0R0008Q3JB | 60.0 micrograms | — |
| Vitamin B12 UNII · 8406EY2OQA | 6.0 micrograms | — |
| Vaccinium myrtillus | 171.0 milligrams | — |
| Vitis vinifera Grape | 42.75 milligrams | — |
| Folate UNII · 935E97BOY8 | 200.0 micrograms | — |
| 1,4-alpha-D-Glucan glucohydrolase | 2.6 FCC Glucoamylase Units | — |
| Vitamin B6 UNII · KV2JZ1BI6Z | 2.0 milligrams | — |
What this product supports · authorized claims
10 authority-backed effects
Rolled up from EFSA / FDA / NIH ODS authorized function claims on this product's active ingredients. Each row shows which ingredients contribute.
- from: Vitamin B12 · Vitamin B6
- from: Vitamin B6
- from: Copper · Vitamin B6
- from: Folate · Vitamin B12 · Vitamin B6
- from: Chromium
- from: Copper
- from: Copper
- from: Vitamin E
- from: Folate · Vitamin B12 · Vitamin B6
- from: Vitamin B6
FDA CAERS · adverse event context
9
consumer-submitted adverse event reports filed with the FDA CFSAN Adverse Event Reporting System mentioning this product or its brand.
CAERS reports are unverified consumer submissions — not adjudicated causality. Large well-known brands accumulate proportionally more reports simply due to broader use. About CAERS →